4-(chloromethyl)-1-methyl-1H-pyrazole hydrochloride → HCID 57383224, Verbindung
Reaktionsgleichung
[Cl:1][C:2]1[CH:7]=[CH:6][C:5]([O:8][C:9]2[CH:14]=[CH:13][C:12]([CH2:15][CH2:16][O:17][C:18]3[CH:23]=[CH:22][NH:21][C:20](=[O:24])[N:19]=3)=[CH:11][CH:10]=2)=[CH:4][C:3]=1[C:25]([F:28])([F:27])[F:26].Cl.Cl[CH2:31][C:32]1[CH:33]=[N:34][N:35]([CH3:37])[CH:36]=1>>[Cl:1][C:2]1[CH:7]=[CH:6][C:5]([O:8][C:9]2[CH:10]=[CH:11][C:12]([CH2:15][CH2:16][O:17][C:18]3[CH:23]=[CH:22][N:21]([CH2:31][C:32]4[CH:33]=[N:34][N:35]([CH3:37])[CH:36]=4)[C:20](=[O:24])[N:19]=3)=[CH:13][CH:14]=2)=[CH:4][C:3]=1[C:25]([F:26])([F:28])[F:27]Komponenten
3
Versuchsvorschrift
The title compound was prepared by a procedure similar to that described for E1 starting with 4-{[2-(4-{[4-chloro-3-(trifluoromethyl)phenyl]oxy}phenyl)ethyl]oxy}-2(1H)-pyrimidinone and 4-(chloromethyl)-1-methyl-1H-pyrazole hydrochloride. LC-MS (ESI): m/z 505 [M+H]+; 4.28 min (ret time).
Aufarbeitung
- custom4.28 min (ret time)
Quellen und Nachweise
- ORD-Eintrag
- ord-9c10a44563b44e34bd98f3b259a195fb
- Quelldatensatz
- uspto-grants-2014_10
- Patentnummer
- US08859573B2
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